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FDA 510(k)

SENTRY RADIOTRANSLUCENT ECG ELECTRODES

K-Number: K962122 · 1996-07-24

ApplicantSentry Medical Products, Inc.
Decision Date1996-07-24
Product CodeDRX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SENTRY RADIOTRANSLUCENT ECG ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Sentry Medical Products, Inc.. It received FDA 510(k) clearance on 1996-07-24 under 510(k) number K962122. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SENTRY RADIOTRANSLUCENT ECG ELECTRODES?

SENTRY RADIOTRANSLUCENT ECG ELECTRODES is a medical device that received FDA 510(k) clearance on 1996-07-24. The listed applicant is Sentry Medical Products, Inc.. The 510(k) number is K962122.

When did SENTRY RADIOTRANSLUCENT ECG ELECTRODES receive FDA 510(k) clearance?

SENTRY RADIOTRANSLUCENT ECG ELECTRODES received FDA 510(k) clearance on 1996-07-24, under 510(k) number K962122.

Who is the listed applicant for SENTRY RADIOTRANSLUCENT ECG ELECTRODES?

The FDA 510(k) record lists Sentry Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SENTRY RADIOTRANSLUCENT ECG ELECTRODES?

The FDA product code for SENTRY RADIOTRANSLUCENT ECG ELECTRODES is DRX.

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Other records listing Sentry Medical Products, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K955636SENTRY DISPOSABLE DISPERSIVE ELECTRODEK942827SENTRY INSERTION TRAYK934000SENTRY AQUEOUS GEL ECG ELECTRODESK935098BABY BOARDK933603LEADWIREK932704PATIENT CABLE

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Related Devices (Code: DRX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K171244PhysiotraceNimbleheart, Inc.K123658BIOMODULE 3-M1Zephyr Technology CorporationK101576CENTERRIDGE DIAGNOSTIC ECG ELECTRODE, CENTERRIDGE MONITORING ECG ELECTRODESTeam Innovations, Inc.K101685IP-SETIntegral Process SasK100129AMBU BLUE SENSOR NEO, AMBU BLUE SENSOR NEO XAmbu A/SK093327INTCO TAB ELECTRODEShanghai Intco Electrode Manufacturing Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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